Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Allantoic cyst
Occasional (5-29%)
Retroperitoneal fibrosis
Very rare (1-4%)
Alstrom syndrome
Occasional (5-29%)
Primary hyperoxaluria, type I
Frequent (30-79%)
Double urethra
Occasional (5-29%)
Marquardt-Loriaux syndrome
Frequent (30-79%)
Stevens-Johnson syndrome
Occasional (5-29%)
Acromegaly
Occasional (5-29%)
Congenital junctional epidermolysis bullosa
Occasional (5-29%)
Bradbury-Eggleston syndrome
Frequent (30-79%)
Chester-type porphyria
Ulcerative cystitis
Very frequent (80-99%)
Deficiency of AMP pyrophorylase
Frequent (30-79%)
Idiopathic retroperitoneal fibrosis
Very rare (1-4%)
Troyer syndrome
Frequent (30-79%)
Acute intermittent porphyria
Very rare (1-4%)
Partial hypoxanthine-guanine phosphoribosyltransferase deficiency
Occasional (5-29%)
PUV - Posterior urethral valve
Very rare (1-4%)
Porphobilinogen deaminase deficiency
Junctional epidermolysis bullosa gravis of Herlitz
Occasional (5-29%)
Polyostotic sclerosing histiocytosis
Very frequent (80-99%)
Fowler's syndrome
Frequent (30-79%)
Malakoplakia
Very frequent (80-99%)
Left renal vein entrapment syndrome
Occasional (5-29%)
Small cell neuroendocrine carcinoma of bladder
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 49650001
- UMLS CUI
- C0013428
- Fully Specified Name
- Dysuria (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.